510(k) K853901 ยท GEX Powered Laser Surgical Instrument
ENDO-LASE CD 40 FOR DERMATOLOGY
| Applicant | Endo Lase, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Feb 19, 1986 |
| Received | Sep 20, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853901
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.